Mutant p53 Aggregates into Prion-like Amyloid Oligomers and Fibrils
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Title
Mutant p53 Aggregates into Prion-like Amyloid Oligomers and Fibrils
Authors
Keywords
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Journal
JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 287, Issue 33, Pages 28152-28162
Publisher
American Society for Biochemistry & Molecular Biology (ASBMB)
Online
2012-06-20
DOI
10.1074/jbc.m112.340638
References
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- (2010) Claudia B. Levy et al. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY
- The role of mutant p53 in human cancer
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- The peculiar interaction between mammalian prion protein and RNA
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- Ligand Binding and Hydration in Protein Misfolding: Insights from Studies of Prion and p53 Tumor Suppressor Proteins†
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- The Transcellular Spread of Cytosolic Amyloids, Prions, and Prionoids
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- Structural evolution of p53, p63, and p73: Implication for heterotetramer formation
- (2009) A. C. Joerger et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- TP53 Mutations in Human Cancers: Origins, Consequences, and Clinical Use
- (2009) M. Olivier et al. Cold Spring Harbor Perspectives in Biology
- Structural Biology of the Tumor Suppressor p53
- (2008) Andreas C. Joerger et al. Annual Review of Biochemistry
- The (1–63) Region of the p53 Transactivation Domain Aggregates In Vitro into Cytotoxic Amyloid Assemblies
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- Prion Protein Complexed to N2a Cellular RNAs through Its N-terminal Domain Forms Aggregates and Is Toxic to Murine Neuroblastoma Cells
- (2008) Mariana P. B. Gomes et al. JOURNAL OF BIOLOGICAL CHEMISTRY
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